Impact of adherence to beta-blockers in all-comers ST-segment elevation myocardial infarction (STEMI) patients and according to left ventricular ejection fraction (LVEF) at discharge: results from the real-world registry FAST-STEMI.

IF 2.6 4区 医学 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS Journal of Cardiovascular Pharmacology Pub Date : 2024-08-29 DOI:10.1097/fjc.0000000000001627
Giuseppe Giannino,Federico Giacobbe,Umberto Annone,Emanuele Ravetti,Cesare Rollo,Marco Nebiolo,Mattia Troncone,Umberto Di Vita,Arianna Morena,Ludovica Carmagnola,Filippo Angelini,Ovidio De Filippo,Francesco Bruno,Corrado Pancotti,Luca Gaido,Piero Fariselli,Prof Fabrizio D'Ascenzo,Massimo Giammaria,Gaetano Maria De Ferrari
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Abstract

Beta-blockers are a crucial part of post-myocardial infarction (MI) pharmacological therapy. Recent studies have raised questions about their efficacy in patients without reduced left ventricular ejection fraction (LVEF). This study aims to assess adherence to beta-blockers after discharge for ST-segment elevation myocardial infarction (STEMI) and the impact of adherence on outcomes based on LVEF at discharge. The retrospective registry FAST-STEMI evaluated real-world adherence to main cardiovascular drugs in STEMI patients between 2012 and 2017 by comparing purchased tablets to expected ones at one year through pharmacy registries. Optimal adherence was defined ≥80%. Primary outcomes included all-cause and cardiovascular death, while secondary outcomes were myocardial infarction, major/minor bleeding events, and ischemic stroke The study included 4688 patients discharged on beta-blockers. Mean age was 64 ± 12.3 years, 76% were male, and mean LVEF was 49.2 ± 8.8%. Mean adherence at one year was 87.1%. Optimal adherence was associated with lower all-cause (adjHR 0.62, 95%CI 0.41-0.92, p 0.02) and cardiovascular mortality (adjHR 0.55, 95%CI 0.26-0.98, p 0.043). In LVEF ≤40% patients, optimal adherence was linked to reduced all-cause and cardiovascular mortality but this was not found either in patients with preserved or mildly reduced LVEF. Predictors of cardiovascular mortality included older age, chronic kidney disease, male gender, and atrial fibrillation. Optimal adherence to beta-blocker therapy in all-comers STEMI patients reduced all-cause and cardiovascular mortality at 1 year; once stratified by LVEF, this effect is confirmed only in patients with reduced LVEF (< 40%) at hospital discharge.
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ST段抬高型心肌梗死(STEMI)患者坚持使用β受体阻滞剂的影响,以及出院时左心室射血分数(LVEF)的情况:FAST-STEMI 真实世界登记的结果。
β-受体阻滞剂是心肌梗死(MI)后药物治疗的重要组成部分。最近的研究对β-受体阻滞剂在左心室射血分数(LVEF)不降低的患者中的疗效提出了质疑。本研究旨在评估ST段抬高型心肌梗死(STEMI)患者出院后是否坚持使用β-受体阻滞剂,以及坚持使用β-受体阻滞剂对基于出院时左心室射血分数(LVEF)的预后的影响。回顾性登记 FAST-STEMI 评估了 2012 年至 2017 年间 STEMI 患者服用主要心血管药物的实际依从性,通过药房登记比较购买药片与一年后的预期药片。最佳依从性定义为≥80%。主要结果包括全因死亡和心血管死亡,次要结果包括心肌梗死、大/小出血事件和缺血性卒中。 研究纳入了4688名使用β受体阻滞剂出院的患者。平均年龄为 64 ± 12.3 岁,76% 为男性,平均 LVEF 为 49.2 ± 8.8%。一年后的平均依从率为 87.1%。最佳依从性与较低的全因死亡率(adjHR 0.62,95%CI 0.41-0.92,p 0.02)和心血管死亡率(adjHR 0.55,95%CI 0.26-0.98,p 0.043)相关。在LVEF≤40%的患者中,最佳依从性与全因死亡率和心血管死亡率的降低有关,但在LVEF保留或轻度降低的患者中却没有发现这种情况。心血管死亡率的预测因素包括年龄较大、慢性肾病、男性和心房颤动。在所有STEMI患者中坚持最佳β受体阻滞剂治疗可降低1年的全因死亡率和心血管死亡率;按LVEF分层后,只有出院时LVEF降低(< 40%)的患者才能证实这种效果。
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来源期刊
CiteScore
5.10
自引率
3.30%
发文量
367
审稿时长
1 months
期刊介绍: Journal of Cardiovascular Pharmacology is a peer reviewed, multidisciplinary journal that publishes original articles and pertinent review articles on basic and clinical aspects of cardiovascular pharmacology. The Journal encourages submission in all aspects of cardiovascular pharmacology/medicine including, but not limited to: stroke, kidney disease, lipid disorders, diabetes, systemic and pulmonary hypertension, cancer angiogenesis, neural and hormonal control of the circulation, sepsis, neurodegenerative diseases with a vascular component, cardiac and vascular remodeling, heart failure, angina, anticoagulants/antiplatelet agents, drugs/agents that affect vascular smooth muscle, and arrhythmias. Appropriate subjects include new drug development and evaluation, physiological and pharmacological bases of drug action, metabolism, drug interactions and side effects, application of drugs to gain novel insights into physiology or pathological conditions, clinical results with new and established agents, and novel methods. The focus is on pharmacology in its broadest applications, incorporating not only traditional approaches, but new approaches to the development of pharmacological agents and the prevention and treatment of cardiovascular diseases. Please note that JCVP does not publish work based on biological extracts of mixed and uncertain chemical composition or unknown concentration.
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